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First report of a FXII gene mutation in a Brazilian family with hereditary angio‐oedema with normal C1 inhibitor
Author(s) -
Stieber C.,
Grumach A.S.,
Cordeiro E.,
ConstantinoSilva R.N.,
Barth S.,
Hoffmann P.,
Pesquero J.B.,
Renné T.,
Nöthen M.M.,
Cichon S.
Publication year - 2015
Publication title -
british journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.304
H-Index - 179
eISSN - 1365-2133
pISSN - 0007-0963
DOI - 10.1111/bjd.13791
Subject(s) - hereditary angioedema , mutation , medicine , c1 inhibitor , genetics , gene , biology , dermatology , angioedema
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